Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07J—STEROIDS
  • C07J63/00—Steroids in which the cyclopenta(a)hydrophenanthrene skeleton has been modified by expansion of only one ring by one or two atoms
  • C07J63/008—Expansion of ring D by one atom, e.g. D homo steroids
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/04—Antibacterial agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/10—Antimycotics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
  • A61P31/14—Antivirals for RNA viruses
  • A61P31/18—Antivirals for RNA viruses for HIV
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P37/00—Drugs for immunological or allergic disorders
  • A61P37/02—Immunomodulators
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
  • C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
  • C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
  • C08B37/0009—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid alpha-D-Glucans, e.g. polydextrose, alternan, glycogen; (alpha-1,4)(alpha-1,6)-D-Glucans; (alpha-1,3)(alpha-1,4)-D-Glucans, e.g. isolichenan or nigeran; (alpha-1,4)-D-Glucans; (alpha-1,3)-D-Glucans, e.g. pseudonigeran; Derivatives thereof
  • C08B37/0012—Cyclodextrin [CD], e.g. cycle with 6 units (alpha), with 7 units (beta) and with 8 units (gamma), large-ring cyclodextrin or cycloamylose with 9 units or more; Derivatives thereof
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
  • C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
  • C08L5/16—Cyclodextrin; Derivatives thereof
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
  • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
  • C07B2200/07—Optical isomers

Definitions

• This invention relates to novel salt forms of 3-O-(3',3'- dimethylsuccinyl) betulinic acid, also known as "DSB".
• This invention also relates to methods of treating H1N and related diseases using pharmaceutical compositions comprising salt forms of DSB.
• the invention further relates to dosage forms of pharmaceutical compositions comprising salts of DSB.
• HIN Human Immunodeficiency Virus
• lentiviruses a subfamily of retroviruses. HIN infects and invades cells of the immune system; it breaks down the body's immune system and renders the patient susceptible to opportunistic infections and neoplasms. The immune defect appears to be progressive and irreversible, with a high mortality rate that approaches 100% over several years.
• HIN-1 is trophic and cytopathic for T4 lymphocytes, cells of the immune system that express the cell surface differentiation antigen CD4, also known as OKT4, T4 and leu3.
• the viral tropism is due to the interactions between the viral envelope glycoprotein, gpl20, and the cell-surface CD4 molecules (Dalgleish et al., Nature 312:763-767, 1984). These interactions, not only mediate the infection of susceptible cells by HIN, but are also HIN-1 is trophic and cytopathic for T4 lymphocytes, cells of the immune system that express the cell surface differentiation antigen CD4, also known as OKT4, T4 and leu3.
• the viral tropism is due to the interactions between the viral envelope glycoprotein, gpl20, and the cell-surface CD4 molecules (Dalgleish et al., Nature 312:763-767, 1984).
• the host range of HIV includes cells of the mononuclear phagocytic lineage (Dalgleish et al., supra), including blood monocytes, tissue macrophages, Langerhans cells of the skin and dendritic reticulum cells within lymph nodes.
• HIN is also neurotropic, capable of infecting monocytes and macrophages in the central nervous system causing severe neurologic damage. Macrophage/monocytes are a major reservoir of HIN. They can interact and fuse with CD4-bearing T cells, causing T cell depletion and thus contributing to the pathogenesis of ADDS.
• Therapeutic agents for HIN can include, but not are not limited to, at least one of AZT, 3TC, ddC, d4T, ddl, tenofovir, abacavir, nevirapine, delavirdine, efavirenz, saquinavir, ritonavir, indinavir, nelfinavir, lopinavir, amprenavir and atazanavir, or any other antiretroviral drugs or antibodies in combination with each other, or associated with a biologically based therapeutic, such as, for example, gp41-derived peptides enfovirtide (Fuzeon; Timeris-Roche), or soluble CD4, antibodies to CD4, and conjugates of CD4 or anti-CD4, or as additionally presented herein. Combinations of these drugs are particularly effective and can reduce levels of viral RNA to undetectable levels in the plasma and slow the development of viral
• Betulinic acid and platanic acid have been isolated from Syzigium claviflorum and were determined to have anti-HJV activity. Betulinic acid and platanic acid exhibited inhibitory activity against HJN-1 replication in H9 lymphocyte cells with EC 50 values of 1.4 ⁇ M and 6.5 ⁇ M, respectively, and therapeutic index (T.I.) values of 9.3 and 14, respectively. Hydrogenation of betulinic acid yielded dihydrobetulinic acid, which showed slightly more potent anti- HIN activity with an EC 50 value of 0.9 and a T.I. value of 14 (Fujioka, T., et al, J. Nat. Prod. 57:243-247 (1994)).
• U.S. Patent No. 5,468,888 discloses 28-amido derivatives of lupanes that are described as having a cytoprotecting effect for HTV-infected cells.
• a number of triterpenoids including betulinic acid, have several known medical applications, including use as an anticancer drug.
• Anderson et al., in WO 95/04526, discuss derivatives of triterpenoids which have been used in cancer therapy, including their activity against polyamines which are required by cells to grow at an optimal rate. Some of these triterpenoids have been found to interfere with the enzymatic synthesis of polyamines required for optimum cell growth, and thus inhibit the growth of cancer cells, particularly by inhibiting ornithine decarboxylase.
• Betulinic acid has been reported also to possess anti-inflammatory activity, which may be due to its capacity to inhibit enzymes involved in leukotriene biosynthesis, including 5- lipoxygenase.
• Japanese Patent Application No. JP 01 143,832 discloses that betulin and 3,28-diesters thereof are useful in the anti-cancer field.
• Ri is a C -C 20 substituted or unsubstituted carboxyacyl
• R 2 is a C 2 -C 20 substituted or unsubstituted carboxyacyl
• R 3 is hydrogen, halogen, amino, optionally substituted mono- or di-alkylamino, or ⁇ OR , where R is hydrogen, C ⁇ _ alkanoyl, benzoyl, or C 2 -C 20 substituted or unsubstituted carboxyacyl; wherein the dashed line represents an optional double bond between C 0 and C 9 .
• Derivatives in U.S. Pat. No. 6,172,110 Bl are formed by introducing a C to C 20 substituted or unsubstituted acyl group at the C3-hydroxy or C28- hydroxy group of betulin and dihydrobetulin to produce the corresponding 3- O-acyl and/or 28- ⁇ -acyl derivatives.
• These compounds were described as usefol for treating a subject infected with a retro viral infection, particularly HIV, by administering at least one of the aforementioned betulin derivatives optionally in combination with one or more known anti-AlDS therapeutic or immunostimulant.
• U.S. Patent Application No. 60/413,451 discloses 3,3-dimethylsuccinyl betulin and is herein incorporated by reference.
• Zhu Y-M. et al, Bioorg. Chem Lett. 77:3115-3118 (2001); Kashiwada Y. et al., J. Nat. Prod. 61:1090- 1095 (1998); Kashiwada Y. et al, J. Nat. Prod. 63:1619-1622 (2000); and Kashiwada Y. et al., Chem. Pharm. Bull.
• the present invention provides therapeutic methods and compounds that inhibit the virus in different ways from approved therapies.
• the present invention provides a therapeutic composition comprising a salt of DSB having enhanced solubility and bioavailability that inhibit the virus in vivo in different ways from approved therapies.
• the compositions of the present invention can be used to treat HIN-1 infection in human beings.
• the compound and methods of the present invention have a novel mechanism of action and therefore are active against HIN strains that are resistant to current therapies. As such, this invention offers a completely new approach for treating HIN/AIDS.
• the present invention relates to particular salt forms of 3-O-(3',3'- dimethylsuccinyl) betulinic acid (“DSB”), their preparation, pharmaceutical compositions thereof, and methods of use thereof.
• this invention relates to amine salts, such as the ⁇ -methyl-D-glucamine ( ⁇ mG) salt form of DSB.
• This invention also relates to pharmaceutical compositions and dosage forms comprising these salt forms of DSB. These compositions and dosage forms can be used in methods of treating HIV and related diseases. Methods of making the salts of DSB and the pharmaceutical compositions are also provided.
• DSB 3-O-(3',3'- dimethylsuccinyl) betulinic acid
• a first aspect of the present invention is directed to a salt form of 3-O- (3 ',3 '-dimethylsuccinyl) betulinic acid, hereinafter 'DSB'.
• DSB has the following formula:
• a second aspect of the present invention is drawn to an NmG salt of DSB.
• the glucamine salt of DSB is the di-(N-methyl-D- glucamine) salt of DSB (di-NmG salt).
• the di-(NmG) salt of DSB can have two NmG molecules bind per DSB molecule, has a molecular formula of C 50 H 90 N O ⁇ 6 , a molecular weight of 975.28 and has the following formula:
• a third aspect of the present invention is drawn to a pharmaceutical composition
• a pharmaceutical composition comprising an NmG salt of DSB, such as the di-(N-methyl-D- glucamine) salt of DSB, and a pharmaceutical carrier or diluent.
• a fourth aspect of the present invention is drawn to a method of preparing an NmG salt of DSB.
• the method of preparing the salt comprises mixing NmG and DSB in an aqueous solution to provide 3-O-(3',3'-dimethylsuccinyl)betulinic acid, N-methyl-D- glucamine salt.
• the mixing can occur in the presence of a cyclodextrin, such as hydroxypropyl- ⁇ -cyclodextrin.
• a fifth aspect of the present invention is drawn to a dosage form, such as an oral tablet, comprising a pharmaceutical composition of an NmG salt of DSB.
• the dosage form can be used for treating, in a subject, a retroviral infection, such as HIV.
• a sixth aspect of the present invention is drawn to a method of use of a pharmaceutical composition comprising an NmG salt of DSB for treating, in a human subject, a retroviral infection, such as HIV.
• Any non-toxic, pharmaceutically acceptable amine or quaternary ammonium salt of DSB can be used in the present invention. These salts can be prepared in situ during the final isolation and purification of the compounds or by separately reacting the purified compound in its free acid form with a suitable organic base and isolating the salt thus formed. These include nontoxic ammonium, quaternary ammonium and amine cations including, but not limited to ammonium, tetra-methylammonium, tetraethylammonium, methylamine, dimethylamine, trimethylamine, ethylamine, N-methyl- glucamine and the like.
• NmG salt form of DSB namely 3-O-(3',3'- dimethylsuccinyl)betulinic acid, N-methyl-D-glucamine salt and the alkali metal salt forms.
• These salt forms have been prepared by combining DSB with NmG or with an alkali metal hydroxide to provide mono- and di-salts of DSB.
• the salt forms of the present invention possess enhanced bioavailability.
• the salts of the present invention have anti-retroviral activity, thus providing suitable compounds and compositions for treating retroviral infections, optionally with additional pharmaceutically active ingredients, such as anti-retroviral, anti-HIV, and/or immuno-stimulating compounds or antiviral antibodies or fragments thereof.
• anti-retroviral activity or "anti-HIV activity” is intended the ability to inhibit at least one of: (1) viral pro-DNA integration into host cell genome; (2) retroviral attachment to cells; (3) viral entry into cells; (4) cellular metabolism which permits viral replication; (5) inhibition of intercellular spread of the virus; (6) synthesis and/or cellular expression of viral antigens; (7) viral budding or maturation; (8) activity of virus-coded enzymes (such as reverse transcriptase, integrase and proteases); and/or (9) any known retroviral or HIV pathogenic actions, such as, for example, immunosuppression.
• any activity which tends to inhibit any of these mechanisms is "anti-retroviral activity” or "anti-HJN activity.”
• a salt of DSB of the present invention can be used for treatment of retroviral (e.g., HIN) infection either alone, or in combination with other modes of therapy known in the art.
• retroviral e.g., HIN
• the salts of DSB of the present invention are relatively less or substantially non-toxic to normal cells, their utility is not limited to the treatment of established retroviral infections.
• a salt of DSB according to the present invention can be used in treating blood products, such as those maintained in blood banks. The nation's blood supply is currently tested for antibodies to HIN. However, the test is still imperfect and samples which yield negative tests can still contain HIN virus. Treating the blood and blood products with the salts of DSB of the present invention can add an extra margin of safety by killing any retrovirus that may have gone undetected.
• a salt of DSB according to the present invention can be used in the treatment of HIN in patients who are not adequately treated by other HJV-1 therapies. Accordingly, the invention is also drawn to a method of treating a patient in need of therapy, wherein the HIN-1 infecting said cells does not respond to other HIN-1 therapies.
• methods of the invention are practiced on a subject infected with an HIN that is resistant to a drug used to treat HIN infection, various applications, the HIN is resistant to one or more protease inhibitors, reverse transcriptase inhibitors, entry inhibitors, nucleoside analogs, vaccines, binding inhibitors, immunomodulators, and/or any other inhibitors, i some embodiments, the compositions and methods of the invention are practiced on a subject infected with an HIN that is resistant to one or more drugs used to treat HIN infections, for example, but not limited to, zidovudine, lamivudine, didanosine, zalcitabine, stavudine, abacavir, nevirapine, delavirdine, emtricitabine, efavirenz, saquinavir, ritonavir, lopinavir, indinavir, nelfinavir, tenofovir, amprenavir, adef
• a salt of DSB of the present invention can be used as a prophylactic to prevent transmission of HIV infection between individuals.
• a salt of DSB can be administered orally or by injection to an HIV infected pregnant woman and/or fetus during pregnancy or immediately prior to, at, or subsequent to birth, to reduce the probability that the newborn infant becomes infected.
• a salt of DSB can be administered vaginally immediately prior to childbirth to prevent infection of the infant during passage through the birth canal.
• a salt of DSB of the present invention can be used during sexual intercourse to prevent transmission of HIV by applying a retroviral inhibiting effective amount of a topical composition including one or more salts of DSB to vaginal or other mucosa prior to sexual intercourse.
• a salt of DSB of the present invention can be used to prevent transmission of HIV from an infected male to an uninfected female or vice versa.
• compositions of the present invention can comprise at least one salt of DSB optionally in combination with one or more additional agent as described herein.
• methods of treatment will employ pharmaceutical compositions that include at least one salt of DSB, as described herein, alone or in combination with additional agents as further described.
• Such modes of therapy can include chemotherapy with at least one additional drug as presented herein.
• a pharmaceutical composition according to the present invention can comprise at least one other anti- viral agents such as, but not limited to, AZT (zidovudine, RETRONIR®, GlaxoSmithKline), 3TC (lamivudine, EPIVIR®, GlaxoSmithKline), AZT+3TC, (COMBINER®, GlaxoSmithKline), AZT+3TC+abacavir (TRIZINIR®, GlaxoSmithKline), ddl (didanosine, VIDEX®, Bristol-Myers Squibb), ddC (zalcitabine, HIVED®, Hoffmann-La Roche), D4T (stavudine, ZERIT®, Bristol-Myers Squibb), tenofovir (VE EAD®, Gilead), abacavir (ZIAGE ⁇ ®, GlaxoSmithKline), nevirapine (VIRAMU ⁇ E®, Boehringer higelheim), delavirdine (AZT (zidovudine
• Additional suitable antiviral agents for optimal use with at least one salt of DSB can include, but are not limited to amphotericin B (FUNGIZONE®); Ampligen (mismatched RNA) developed by Hemispherx Biopharma; BETASERON® ( ⁇ -interferon, Chiron); butylated hydroxytoluene; Carrosyn (polymannoacetate); Castanospermine; Contracan (stearic acid derivative); Creme Pharmatex (containing benzalkonium chloride); 5- unsubstituted derivative of zidovudine; penciclovir (DENAVER.® ⁇ ovartis); famciclovir (FAMNIR® ⁇ ovartis); acyclovir (ZOVE AX® GlaxoSmithKline); cytofovir (VISTTDE® Gilead); ganciclovir (CYTOVE ⁇ E®, HoffmanLaRoche); dextran sulfate; D-penicillamine (3- mercapto-D
• compositions of the present invention can also further comprise immunomodulators.
• Suitable immunomodulators for optional use with a betulinic acid or betulin derivative of the present invention in accordance with the present invention can include, but are not limited to: ABPP (Bropririmine); Ampligen (mismatched RNA, Hemispherx Biopharma); anti-human interferon- ⁇ -antibody; ascorbic acid and derivatives thereof; interferon- ⁇ ; Ciamexon; cyclosporin; cimetidine; CL-246,738; colony stimulating factors, including GM-CSF; dinitrochlorobenzene; HE2000 (Hollis-Eden Pharmaceuticals); inteferon- ⁇ ; glucan; hyperimmune gamma- globulin (Bayer); immuthiol (sodium diethylthiocarbamate); interleukin-1 (Hoffmann-LaRoche; Amgen), interleukin-2 (E -2) (Chiron); isoprinos
• compositions of the present invention can also further comprise anti-cancer therapeutic agents.
• Suitable anti-cancer therapeutic agents for optional use include an anti-cancer composition effective to inhibit neoplasia comprising a compound, or a pharmaceutically acceptable salt or prodrug of said anti-cancer agent, which can be used for combination therapy include, but are not limited to, alkylating agents, such as busulfan, cis-platin, mitomycin C, and carboplatin antimitotic agents, such as colchicine, vinblastine, taxols, such as paclitaxel (TAXOL®, Bristol-Meyers Squibb) docetaxel (TAXOTERE®, Aventis), topo I inhibitors, such as camptothecin, irinotecan and topotecan (HYCAMTIN®, GlaxoSmithKline), topo II inhibitors, such as doxorubicin, daunorubicin and etoposides such as VP16; RNA/DNA anti
• the invention further provides methods for providing anti-bacterial therapeutics, anti-parasitic therapeutics, and anti-fungal therapeutics, for use in combination with the compounds of the invention and pharmaceutically- acceptable salts thereof.
• anti-bacterial therapeutics include compounds such as penicillins, ampicillin, amoxicillin, cyclacillin, epicillin, methicillin, nafcillin, oxacillin, cloxacillin, dicloxacillin, flucloxacillin, carbenicillin, cephalexin, cepharadine, cefadoxil, cefaclor, cefoxitin, cefotaxime, ceftizoxime, cefinenoxine, ceftriaxone, moxalactam, imipenem, clavulanate, timentin, sulbactam, erythromycin, neomycin, gentamycin, streptomycin, metronidazole, chloramphenicol, clindamycin, lincomycin
• anti-parasitic therapeutics include bithionol, diethylcarbamazine citrate, mebendazole, metrifonate, niclosamine, niridazole, oxamniquine and other quinine derivatives, piperazine citrate, praziquantel, pyrantel pamoate and thiabendazole, as well as derivatives and altered forms of each of these compounds.
• anti-fungal therapeutics include amphotericin B, clotrimazole, econazole nitrate, flucytosine, griseofolvin, ketoconazole and miconazole, as well as derivatives and altered forms of each of these compounds.
• Anti-fungal compounds also include aculeacin A and papulocandin B.
• a preferred animal subject of the present invention is a human being.
• the present invention is usefol in the treatment of human patients.
• treating means the administering to subjects a salt of DSB according to the present invention for purposes which can include prevention, amelioration, or cure of a retroviral-related pathology.
• Medicaments are considered to be provided "in combination" with one another if they are provided to the patient concurrently or if the time between the administration of each medicament is such as to permit an overlap of biological activity.
• a pharmaceutical composition comprises the di-(N-methyl-D-glucamine) salt of 3-O-(3',3'- dimethylsuccinyl)betulinic acid.
• compositions for administration according to the present invention comprising at least one salt of DSB according to the present invention in a pharmaceutically acceptable form are optionally combined with a pharmaceutically acceptable carrier. These compositions can be administered by any means that achieve their intended purposes. Amounts and regimens for the administration of the salts of DSB according to the present invention can be determined readily by those with ordinary skill in the clinical art of treating a retroviral pathology.
• administration can be by parenteral, such as subcutaneous, intravenous, intramuscular, intraperitoneal, transdermal, or buccal routes. Alternatively, or concurrently, administration can be by the oral route.
• the dosage administered depends upon the age, health and weight of the recipient, type of previous or concurrent treatment, if any, frequency of treatment, and the nature of the effect desired.
• Compositions within the scope of this invention include all compositions comprising at least one salt of DSB according to the present invention in an amount effective to achieve its intended purpose. While individual needs vary, determination of optimal ranges of effective amounts of each component is within the skill of the art.
• Typical dosages of at least one salt of DSB comprise about 0.05 to about 100 mg/kg body weight, hi some embodiments, a usefol dosage of one or more salts of DSB comprises about 0.1 to about 100 mg/kg body weight of the active ingredient, preferably about 0.1 to about 20 mg/kg body weight of the active ingredient. In some embodiments, a more preferred dosage of one or more salts of DSB comprises about 0.2 to about 10 mg/kg body weight. A usefol dosage of one or more salts of DSB comprises about 0.5 to about 5 mg/kg body weight, hi some embodiments, the dosage of one or more salts of DSB can comprise about 10 to about 100 mg/kg body weight.
• a preferred dosage amount is one which provides a trough concentration of DSB in the patient's plasma of about 1 micromolar ( ⁇ M) to about 1 millimolar (mM).
• the dosage amount is one which provides a trough concentration of DSB in the patient's plasma of about 4 ⁇ M (2.34 ⁇ g/mL) to about 1000 ⁇ M, about 40 ⁇ M to about 1000 ⁇ M, or about 400 ⁇ M to about 1000 ⁇ M.
• the dosage amount is one which provides a trough concentration of DSB in the patient's plasma of about 4 ⁇ M (2.34 ⁇ g/mL) to about 200 ⁇ M, about 10 ⁇ M to about 200 ⁇ M, or about 40 ⁇ M to about 200 ⁇ M.
• the dosage amount is one which provides a trough concentration of DSB in the patient's plasma of at least about 4 ⁇ M (2.34 ⁇ g/mL) or greater, at least about 10 ⁇ M or greater, at least about 40 ⁇ M or greater, at least about 100 ⁇ M or greater, or at least 200 ⁇ M or greater.
• the dosage amount is one which provides a trough concentration of DSB in the patient's plasma of about 400 ⁇ M.
• the "trough concentration” is the concentration of DSB in the patient's plasma just prior to subsequent dosing of the patient.
• Therapeutic administration can also include prior, concurrent, subsequent or adjunctive administration of at least one additional salt of DSB according to the present invention or other therapeutic agent, such as an antiviral or immune stimulating agent, hi such an approach, the dosage of the second drug can be the same as or different from the dosage of the first therapeutic agent.
• the drugs are administered on alternate days in the recommended amounts of each drug.
• a pharmaceutical composition of the present invention can also contain suitable pharmaceutically acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which can be used pharmaceutically.
• the preparations particularly those preparations which can be administered orally, such as tablets, dragees, and capsules, and also preparations which can be administered rectally, such as suppositories, as well as suitable solutions for administration by injection or orally, contain from about 0.01 to 99 percent of the active ingredient together with the excipient.
• the preparation can include from about 20 to 75 percent of active compound(s), together with the excipient.
• compositions of the present invention are manufactured in a manner which is itself known, for example, by means of conventional mixing, granulating, dragee-making, dissolving, or lyophilizing processes.
• pharmaceutical preparations for oral use can be obtained by combining the active compounds with solid excipients, optionally grinding the resulting mixture, and processing the mixture of granules, after adding suitable auxiliaries, if desired or necessary, to obtain tablets or dragee cores.
• Suitable excipients are, e.g., fillers such as saccharide, for example, lactose or sucrose, mannitol or sorbitol; cellulose preparations and/or calcium phosphates, such as tricalcium phosphate or calcium hydrogen phosphate; as well as binders such as starch paste, using, for example, maize starch, wheat starch, rice starch, potato starch, gelatin, tragacanth, methyl cellulose, hydroxypropylmethylcellulose, sodium carboxymethylcellulose, and/or polyvinyl pyrrohdone.
• fillers such as saccharide, for example, lactose or sucrose, mannitol or sorbitol
• cellulose preparations and/or calcium phosphates such as tricalcium phosphate or calcium hydrogen phosphate
• binders such as starch paste, using, for example, maize starch, wheat starch, rice starch, potato starch, gelatin, tragacanth, methyl
• disintegrating agents can be added such as the above-mentioned starches and also carboxymethyl starch, cross-linked polyvinyl pyrrohdone, agar, or alginic acid or a salt thereof, such as sodium alginate.
• Auxiliaries are, above all, flow-regulating agents and lubricants, for example, silica, talc, stearic acid or salts thereof, such as magnesium stearate or calcium stearate, and/or polyethylene glycol.
• Dragee cores are provided with suitable coatings which, if desired, are resistant to gastric juices.
• concentrated saccharide solutions can be used, which can optionally contain gum arabic, talc, polyvinyl pyrrohdone, polyethylene glycol and/or titanium dioxide, lacquer solutions and suitable organic solvents or solvent mixtures.
• suitable cellulose preparations such as acetylcellulose phthalate or hydroxypropylmethyl cellulose phthalate are used.
• Dyestuffs or pigments can be added to the tablets or dragee coatings, for example, for identification or in order to characterize combinations of active compound doses.
• Other pharmaceutical preparations which can be used orally include push-fit capsules made of gelatin, as well as soft, sealed capsules made of gelatin and a plasticizer such as glycerol or sorbitol.
• the push-fit capsules can contain the active compounds in the form of granules which can be mixed with fillers such as lactose, binders such as starches, and/or lubricants such as talc or magnesium stearate and, optionally, stabilizers.
• the active compounds can be dissolved or suspended in suitable liquids, such as fatty oils or liquid paraffin, hi addition, stabilizers can be added.
• Possible pharmaceutical preparations which can be used rectally include, for example, suppositories which consist of a combination of the active compounds with a suppository base.
• Suitable suppository bases are, for example, natural or synthetic triglycerides, or paraffin hydrocarbons, addition, it is also possible to use gelatin rectal capsules which consist of a combination of the active compounds with a base.
• Possible base materials include, for example, liquid triglycerides, polyethylene glycols, or paraffin hydrocarbons.
• Suitable formulations for parenteral administration include aqueous solutions of the active compounds in water-soluble form, for example, water- soluble salts.
• suspensions of the active compounds as appropriate oily injection suspensions can be administered.
• Suitable lipophilic solvents or vehicles include fatty oils, such as sesame oil, or synthetic fatty acid esters, such as ethyl oleate or triglycerides.
• Aqueous injection suspensions that can contain substances which increase the viscosity of the suspension include, for example, sodium carboxymethyl cellulose, sorbitol, and/or dextran.
• the suspension can also contain stabilizers.
• Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, solutions, suspensions, syrups, and elixirs, a addition to the active compounds, the liquid dosage forms may contain inert diluents commonly used in the art such as, for example, water or other solvents, solubilizing agents and emulsifiers such as, for example, water or other solvents, solubilizing agents and emulsifiers such as ethyl alcohol, isopropyl alcohol, cyclodextrins such as hydroxypropyl- ⁇ -cyclodextrin, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, dimethyl formamide, oils such as cottonseed, groundnut, corn, germ, olive, castor, and sesame oils, glycerol, tetrahydroforfuryl alcohol, polyethylene glycols and
• Suspensions in addition to the active compounds, may contain suspending agents as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, cellulose, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar, and tragacanth, and combinations thereof.
• suspending agents as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, cellulose, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar, and tragacanth, and combinations thereof.
• a pharmaceutical formulation for systemic administration according to the invention can be formulated • for enteral, parenteral or topical administration. Indeed; all three types of formulation can be used simultaneously to achieve systemic administration of the active ingredient.
• Suitable formulations for oral administration include oral dosage forms such as, but not limited to, hard or soft gelatin capsules, dragees, pills, tablets, including coated tables, elixirs, suspensions, syrups or inhalations and controlled release forms thereof.
• Solid dosage forms in addition to those formulated for oral administration include rectal suppositories.
• the salts of DSB of the present invention can also be administered in the form of an implant when compounded with a biodegradable slow-release carrier.
• the salts of DSB of the present invention can be formulated as a transdermal patch for continuous release of the active ingredient.
• Suitable formulations for topical administration include creams, gels, jellies, mucilages, pastes and ointments.
• Suitable mjectable solutions include intravenous subcutaneous and intramuscular injectable solutions.
• the salts of DSB can be administered in the form of an infosion solution, a nasal inhalation or spray, or a mucosal or vaginal delivery system, such as a vaginal ring, foam, cream, gel, medicated suppository and medicated tampon.
• Prophylactic topical compositions for preventing HIV infection between individuals during childbirth or sexual intercourse include one or more salts of DSB and at least one pharmaceutically acceptable topical carrier or diluent.
• the topical composition can be, for example, in the form of an ointment, a cream, a gel, a lotion, a paste, a jelly, a spray, a foam, or a sponge.
• the dosage amount of a salt of DSB in a prophylactic topical formulation is, in general, less than about 1,000 milligrams, and in some embodiments between about 0.01 to about 100 milligrams.
• the topical formulations can include other prophylactic ingredients.
• the carrier and diluents should be acceptable in the sense of being compatible with other ingredients of the formulation and not deleterious to the recipient.
• Topical prophylactic formulations include those suitable for vaginal, rectal or topical administration.
• the formulations can, where appropriate, be conveniently presented in discrete dosage units, and can be prepared by any of the methods known in the art of pharmacy. All such methods include the step of bringing the active agent into association with liquid carriers, gels or finely divided solid carriers or both and then, if necessary, shaping the product into the desired formulation.
• Prophylactic formulations suitable for vaginal administration can be presented as pessaries, tampons, creams, gels, pastes, jelly, foams, or sprays, or aqueous or oily suspensions, solutions or emulsions (liquid formulations) containing suitable carriers known in the art in addition to the active agent.
• Liquid formulations can contain conventional additives, such as, suspending agents, emulsifying agents, non-aqueous vehicles including edible oils, or preservatives. These formulations are usefol to prevent both sexual transmission of HIV and infection of an infant during passage through the birth canal.
• the vaginal administration can take place prior to sexual intercourse, or immediately prior to childbirth.
• prophylactic formulations suitable for rectal or vaginal administration having a solid carrier are represented as unit dose suppositories.
• Suitable carriers include cocoa butter and other materials commonly used in the art.
• Suppositories can be formed, for example, mixing one or more salts of DSB with one or more softened or melted carriers followed by chilling and shaping in molds.
• Prophylactic formulations according to the invention can also be in the form of drops formulated with an aqueous or non-aqueous base comprising one or more dispersing agents, solubilizing agents, or suspending agents.
• Liquid sprays can be delivered from pressurized packs.
• Prophylactic formulations according to the invention can be adapted to give sustained delivery.
• the prophylactic formulations can include other active agents, such as spermicidal agents, antimicrobial agents, and anti-viral agents.
• the triterpene derivatives of the present invention can also be administered in the form of an implant when compounded with a biodegradable slow-release carrier.
• the triterpene derivatives of the present invention can be formulated as a transdermal patch for continuous release of the active ingredient.
• Salts of the present invention are made by mixing a basic or cation- forming compound, such as NmG, and DSB in an aqueous solution.
• the mixing can occur in the presence of a cyclodextrin, such as hydroxypropyl- ⁇ - cyclodextrin.
• the free acid of DSB can be obtained by the synthesis method described in U.S. Patent No. 5,679,828.
• DSB-(NmG) 2 The solubility of the DSB-(NmG) 2 as a function of pH was measured at 25°C.
• DSB-(NmG) 2 was visibly soluble in basic and neutral conditions.
• a solubility of 7.537 mg/mL was observed at a pH of 9.461, and a solubility of 7.463 mg/mL was observed at a pH of 10.691.
• DSB-(NmG) 2 was visually insoluble in strongly acid solutions at 25°C.
• the objective of this study was to compare the pharmacokinetics of various formulations of DSB administered as the free acid or as one of the salt forms: NmG, Na, or K.
• a solution or suspension of the free acid or salt was administered by oral gavage using a feeding needle to provide a nominal oral dose of 25 mg/kg.
• the dose administered was based on free acid equivalents.
• the group number and formulations are listed below.
• Group 1 25 mg/mL DSB free acid in 2% DMA (dimethylacetamide), 14% Vitamin E TPGS, 84% Captex (a diester formed from selected high purity vegetable fatty acids and propylene glycol (triglyceride))
• Group 2 25 mg/mL of the DSB free acid in 4% Vitamin E TPGS and 96% carboxymethylcellulose (CMC) (0.5%) suspension in water.
• CMC carboxymethylcellulose
• Group 3 41.7 mg/mL of DSB-(NmG) 2 salt in 84% water, 4% ethanol, and 12% PEG 400 (equivalent to 25 mg/mL of free acid)
• Group 4 41.7 mg/mL of the DSB-(NmG) 2 salt in 84% water, 4% ethanol, and 10% PEG 400, 2% Vitamin E TPGS (equivalent to 25
• Group 5 41.7 mg/mL of the DSB-(NmG) 2 salt in 10% hydroxy- ⁇ - cyclodextrin in water (equivalent to 25 mg/mL of free acid)
• Group 6 25 mg/mL of the micronized DSB free acid in 0.5% CMC suspension
• Group 7 25 mg/mL of the micronized DSB free acid in 0.5% CMC suspension and Vitamin E TPGS
• Group 8 28.3 mg/mL of the DSB-K 2 salt inl0% hydroxy- ⁇ -cyclodextrin in water (equivalent to 25 mg/mL of free acid)
• Group 9 13.5 mg/mL of the DSB-(Na) 2 salt in 10% hydroxy- ⁇ - cyclodextrin in water (equivalent to 12.5 mg/mL of free acid)
• the results of this study are presented in Table 5.
• the results of this study are presented in Table 5.
• the NmG salt formulations had the highest oral bioavailability, ranging from 49%-71%.
• the data for Groups 5, 8 and 9 show that, at equivalent doses, the rank order of bioavailability of the salts is NmG > potassium > sodium in a solvent of 10% hydroxypropyl- ⁇ - cyclodextrin in water.
• Bioavailability was calculated as the dose-adjusted ratio of AU NF obtained after oral versus intravenous administration of
• mice Male C.B-17 SCED mice were obtained at 6 weeks of age and implanted with human fetal tissue from a single donor. At 14 weeks, mice were implanted with fragments of human fetal liver and human fetal thymus under the mouse kidney capsule to create the SCED-hu Thy/Liv mice. When the implants reached approximately 30 mm the animals were entered into the experiment. Inoculations of SCED-hu Thy/Liv mice with HIV-1 were performed on anesthetized mice in a restricted animal barrier facility under BSL3 guidelines.
• Thy/Liv implant was injected with 50 ⁇ L (1,000 TCDD50) of NL4-3 batch JK WS1 D3 (diluted 1:2) or with RPMI 1640 medium in 1 to 3 places with a 250- ⁇ L Hamilton glass syringe and 30-gauge x 1/2-inch blunt needle.
• implants were inoculated 18 weeks after tissue implantation. All implants were collected 21 days after inoculation.
• the dosing vehicle was 10% hydroxypropyl- ⁇ -cyclodextrin in sterile PBS (phosphate buffered saline). Dosing solutions were prepared fresh before each administration at concentrations of 12 and 38 mg/mL for dosing at 100 and 300 mg/kg/day of DSB free acid.
• mice were dosed orally by gavage (200 ⁇ L/dose) twice per day and observed for signs of toxicity. Because toxicity was observed in mice treated at 300 mg/kg/day, the dosage level was reduced to 150 mg/kg/day beginning 7 days after treatment initiation after recovery period of 5 days without treatment. Treated mice were observed at the time dosing for signs of toxicity and were weighed every 2-5 days. Mice were inoculated with NL4-3 one day after the first dose (1-2 hr after the AM dose), and dosing was performed for 22 days.
• Thy/Liv implants were surgically excised and transferred into 6-well tissue culture plates containing cold sterile PBS/2% FBS (fetal bovine serum).
• FBS fetal bovine serum
• a single cell suspension was made by placing the implant into a sterile nylon mesh bag, submerging the bag in PBS/2% FBS in a 60-mm tissue culture dish, and dispersing the tissue between the nylon layers with forceps. The cells were counted with a Coulter counter, and appropriate numbers of cells were aliquoted for each assay.
• pellets of 2.5 x 10 6 cells were resuspended in 400 ⁇ L of p24 lysis buffer, rotated overnight at 4 °C, and stored at -20 °C.
• RNA quantitation by branched DNA assay dry pellets of 5 x 10 cells were frozen and stored at - 80 °C.
• FACS analysis 10 6 cells per well were placed in a 96-well plate for fixation and staining and were analyzed on the same day by four-color FACS analysis.
• All three salts of DSB exhibited significantly higher water solubility than the free acid (-100 ⁇ g/mL).
• the NmG salt of DSB was demonstrably more soluble in a solution of 10% hydroxypropyl- ⁇ -cyclodextrin in water than both the potassium and sodium salts.
• the rat bioavailability study evaluated the three salt forms of DSB in five different formulations (three with NmG, one with sodium, and one with potassium) and five different formulations containing the free acid.
• the NmG salt formulations had the highest oral bioavailability, ranging from 49%-71%.
• the SCED-Hu mouse study demonstrated that DSG-(NmG) is a potent in vivo inhibitor of HIN-1 replication.

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